- Author:
	        		
		        		
		        		
			        		Byung Hwa PARK
			        		
			        		
			        		
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			        		;
		        		
		        		
		        		
			        		Ye Na KIM
			        		
			        		;
		        		
		        		
		        		
			        		Ho Sik SHIN
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Review Article
 - From: Clinical Transplantation and Research 2024;38(1):1-6
 - CountryRepublic of Korea
 - Language:English
 - Abstract: Following kidney transplantation, antibody-mediated rejection (AMR) occurs when the antibodies of the immune system attack the transplanted organ, leading to damage of the kidney tissue. De novo human leukocyte antigen donor-specific antibodies (HLADSAs) play a key role in AMR. Current therapeutic approaches include intravenous immunoglobulin, anti-CD20 antibodies, and plasmapheresis. In cases resistant to treatment, proteasome inhibitors and C5 inhibitors may be employed. Nevertheless, a pressing need exists for new medications to improve transplant survival and reduce complications. In the context of AMR, interleukin (IL)-6 is instrumental in the development and maturation of B cells into plasma cells, which then produce HLA-DSAs targeting the allograft. IL-6 inhibitors are currently under investigation and show promise due to the essential role of IL-6 in the immune response; however, additional research is necessary.
 
            
